Voltage-dependent block of the cystic fibrosis transmembrane conductance regulator Cl- channel by two closely related arylaminobenzoates
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Regulation of CFTR chloride channels by syntaxin and Munc18 isoformsInhibition of cAMP-activated intestinal chloride secretion by diclofenac: cellular mechanism and potential application in choleraEvidence for KCNQ1 K+ channel expression in rat zymogen granule membranes and involvement in cholecystokinin-induced pancreatic acinar secretionPerturbation of the pore of the cystic fibrosis transmembrane conductance regulator (CFTR) inhibits its atpase activity.Epac1 mediates protein kinase A-independent mechanism of forskolin-activated intestinal chloride secretion.Electrophysiological evidence for the presence of cystic fibrosis transmembrane conductance regulator (CFTR) in mouse sperm.Three charged amino acids in extracellular loop 1 are involved in maintaining the outer pore architecture of CFTR.Flufenamic acid as an ion channel modulator.The tyrosine kinase p60c-src regulates the fast gate of the cystic fibrosis transmembrane conductance regulator chloride channelCystic fibrosis transmembrane conductance regulator (CFTR) anion binding as a probe of the poreInteraction between permeation and gating in a putative pore domain mutant in the cystic fibrosis transmembrane conductance regulator.CFTR and calcium-activated chloride channels in primary cultures of human airway gland cells of serous or mucous phenotypeThe block of CFTR by scorpion venom is state-dependentCystic fibrosis transmembrane conductance regulator chloride channel blockers: Pharmacological, biophysical and physiological relevance.Substrates of multidrug resistance-associated proteins block the cystic fibrosis transmembrane conductance regulator chloride channel.Inhibition of heterologously expressed cystic fibrosis transmembrane conductance regulator Cl- channels by non-sulphonylurea hypoglycaemic agents.A mouse model for the delta F508 allele of cystic fibrosis.Nanomolar CFTR inhibition by pore-occluding divalent polyethylene glycol-malonic acid hydrazidesChloride secretion by cultures of pig tracheal gland cells.In vivo activation of the cystic fibrosis transmembrane conductance regulator mutant deltaF508 in murine nasal epitheliumNiflumic acid inhibits chloride conductance of rat skeletal muscle by directly inhibiting the CLC-1 channel and by increasing intracellular calcium.A G protein-gated K channel is activated via beta 2-adrenergic receptors and G beta gamma subunits in Xenopus oocytes.Locating the anion-selectivity filter of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel.Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions.Multi-Ion mechanism for ion permeation and block in the cystic fibrosis transmembrane conductance regulator chloride channelProbing an open CFTR pore with organic anion blockersCFTR: covalent and noncovalent modification suggests a role for fixed charges in anion conduction.Positioning of extracellular loop 1 affects pore gating of the cystic fibrosis transmembrane conductance regulatorHCO3-dependent pHi regulation in tracheal epithelial cells.Biophysical and pharmacological characterization of hypotonically activated chloride currents in cortical astrocytesCLC-0 and CFTR: chloride channels evolved from transporters.Modulators of ion transport in nasal polyps: an in situ measurement of short-circuit current.Syntaxin 1A is expressed in airway epithelial cells, where it modulates CFTR Cl(-) currents.Aqueous cigarette smoke extract induces a voltage-dependent inhibition of CFTR expressed in Xenopus oocytes.An Exploration of Charge Compensating Ion Channels across the Phagocytic Vacuole of Neutrophils.The second half of the cystic fibrosis transmembrane conductance regulator forms a functional chloride channel.Connexin Hemichannels in Astrocytes: An Assessment of Controversies Regarding Their Functional Characteristics.Inhibitors of connexin and pannexin channels as potential therapeutics.Polystyrene nanoparticles activate ion transport in human airway epithelial cells.Blockers of VacA provide insights into the structure of the pore.
P2860
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P2860
Voltage-dependent block of the cystic fibrosis transmembrane conductance regulator Cl- channel by two closely related arylaminobenzoates
description
1993 nî lūn-bûn
@nan
1993 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Voltage-dependent block of the ...... ely related arylaminobenzoates
@ast
Voltage-dependent block of the ...... ely related arylaminobenzoates
@en
Voltage-dependent block of the ...... ely related arylaminobenzoates
@nl
type
label
Voltage-dependent block of the ...... ely related arylaminobenzoates
@ast
Voltage-dependent block of the ...... ely related arylaminobenzoates
@en
Voltage-dependent block of the ...... ely related arylaminobenzoates
@nl
prefLabel
Voltage-dependent block of the ...... ely related arylaminobenzoates
@ast
Voltage-dependent block of the ...... ely related arylaminobenzoates
@en
Voltage-dependent block of the ...... ely related arylaminobenzoates
@nl
P2093
P3181
P356
P1476
Voltage-dependent block of the ...... ely related arylaminobenzoates
@en
P2093
J R Riordan
N A McCarty
N Davidson
S McDonough
P3181
P356
10.1085/JGP.102.1.1
P407
P50
P577
1993-07-01T00:00:00Z